Canonical Allele Identifier: CA448707658
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225684G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225450G>T , CM000668.2:g.3225450G>T GRCh38
NC_000006.11:g.3225684G>T , CM000668.1:g.3225684G>T GRCh37
NC_000006.10:g.3170683G>T NCBI36
NG_016715.1:g.7285C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.639C>A MANE Select ENSP00000259818.6:p.Arg213=
ENST00000680070.1:n.1569C>A
ENST00000681707.1:n.1466C>A
ENST00000681757.1:n.944C>A
ENST00000259818.7:c.639C>A ENSP00000259818.6:p.Arg213=
ENST00000473006.1:n.756C>A
NM_178012.4:c.639C>A NP_821080.1:p.Arg213=
XM_011514571.1:c.423C>A XP_011512873.1:p.Arg141=
NM_178012.5:c.639C>A MANE Select NP_821080.1:p.Arg213=